Novel metallized dyes, their manufacture and use

Abstract

The present invention relates to copper, nickel, chromium or cobalt complexes of azo or azomethine dyes which contain a group of the formula--N.dbd.N.dbd.Ar).sub.m-1 Z--R.sub.2 --Uwherein Z is a bridge member of the formula ##STR1## wherein R.sub.1 is hydrogen or a low molecular alkyl group, R.sub.2 is a low molecular alkylene radical or an arylene radical, Ar is an arylene radical, m is 1 or 2 and U is a sulpho or carboxy group.

Description

The present invention provides copper, nickel, chromium and cobalt complexes of azo or azomethine dyes of the formula ##STR2## wherein D is a radical of the benzene or naphthalene class, X is a nitrogen atom or the CH group, Y is the OH, OCH.sub.3 or COCH group, Y' is the OH group, the OCH.sub.3 group or is an amino group, but Y and Y' may not both be the methoxy group, and wherein E, if X is a nitrogen atom, is the radical of a coupling component of the phenol, naphthol or naphthylamine class, of the 5-hydroxypyrazole, 5-aminopyrazole, acetoacetanilide, 2,4-dioxyquinoline or 6-hydroxy-pyridone class or is the radical of a 2,4-diamino-5-cyano- or -5-carbonamidopyridine which carries in 6-position a substituted or an unsubstituted amino, alkoxy, aryloxy, alkylmercapto or arylmercapto group, and, if X is the methine group, E is the radical of a o-hydroxybenzaldehyde or o-hydroxynaphthaldehyde, and wherein one of the radicals D or E contains a group of the formula

--N.dbd.N.dbd.Ar).sub.m-1 Z--R.sub.2 --U (2)

wherein Z is a bridge member of the formula ##STR3## wherein R.sub.1 is hydrogen or a low molecular alkyl group, R.sub.2 is a low molecular alkylene radical or an arylene radical, Ar is an arylene radical, m is 1 or 2 and U is a sulpho or carboxy group, and wherein D and E, besides carrying this group, can carry the customary non-ionogenic substituents which do not impart solubility in water and together can carry at most one additional sulpho group.

The sulpho and carboxy groups can of course also be in ionised form, e.g. as alkali or ammonium sulphonates or carboxylates. For the sake of simplicity, however, the dyes will always be described herein in the form of the free acids.

These complexes are manufactured by reacting an azo or azomethine compound of the formula (1) in the ratio 1:1 with copper, nickel or chromium donors or in the ratio 1:2 with chrommium or cobalt donors.

Y is above all the hydroxy or carboxy group and Y' is also preferably hydroxy. If Y' is an amino group, it is primarily the NH.sub.2 or a low molecular NH-alkyl group. The term "low molecular" denotes herein radicals of 1 to 4 carbon atoms.

The term "arylene" denotes substituted or unsubstituted naphthylene and especially phenylene radicals. Examples of suitable substituents thereof are halogen atoms, in particular chlorine, and low molecular alkyl and alkoxy groups, such as methyl and methoxy, R.sub.2 in the significance of an arylene radical is preferably phenylene.

The present invention provides above all the copper and nickel complexes of azo dyes of the formula ##STR4## wherein p is 1 or 2 and D and E have the meanings previously assigned to them and wherein the radical of the formula (2) is bonded to the diazo component D.

The azo and azomethine compounds of the formulae (1) and (8) are obtained in known manner by coupling or condensation of an amine with an aldehyde.

The radical D is derived from an aminophenol or aminonaphthol or from the corresponding methoxy compounds or from an anthranilic acid, and, besides the group of the formula (2), can carry in addition one or two of the following substituents: chlorine, bromine, nitro, trifluoromethyl, low molecular alkyl and low molecular alkoxy.

Suitable aromatic amines from which D is derived are:

2-amino-1-hydroxybenzene-4- or -5-(N-(o-sulphophenyl)-sulphonamide

2-amino-1-carboxybenzene-4- or -5-(N-(p-sulphophenyl)-sulphonamide

2-amino-1-hydroxybenzene-5-N-methyl-N-(p-sulphophenyl)-sulphonamide

2-amino-1-methoxybenzene-4-N-(m-sulphophenyl)-sulphonamide

4-nitro- or 4-chloro-2-amino-1-hydroxybenzene-5-N-(.beta.-sulphoethyl)-sulphonamide

6-chloro-2-amino-1-hydroxybenzene-4-N-(.gamma.-sulphopropyl)-sulphonamide

6- or 5-nitro-2-amino-1-hydroxybenzene-4-N-(sulphomethyl)-sulphonamide

1-amino-2-hydroxynaphthalene-6-N-(p-sulphophenyl)-sulphonamide

1-amino-2-methoxynaphthalene-6-N-(p-sulphophenyl)-sulphonamide

2-amino-1-hydroxynaphthalene-3-N-(.beta.-sulphoethyl)-sulphonamide

2-amino-1-hydroxynaphthalene-4-N-(.beta.-sulphoethyl)-sulphonamide

2-amino-1-hydroxynaphthalene-6-N-(o-sulphophenyl)-sulphonamide

2-amino-1-carboxybenzene-4- or -5-(o-carboxyphenyl)-sulphonamide

2-amino-1-hydroxybenzene-4-N-(o-carboxyphenyl)-sulphonamide

2-amino-1-hydroxybenzene-5-(o-sulphophenyl)-sulphone.

If the coupling component contains the group of the formula(2), then suitable diazo components are also e.g. the following amines:

anthranilic acid

3- or 5-chloroanthranilic acid

2-amino-1-methoxybenzene

4-chloro- and 4,6-dichloro-2-amino-1-hydroxybenzene

4- or 5-nitro-2-amino-1-hydroxybenzene

4-methoxy-2-amino-1-hydroxybenzene

4-methyl-2-amino-1-hydroxybenzene

The radical E can be derived from the following groups of coupling components:

1- or 2-naphthols which are substituted by chlorine, bromine, acylamino, low molecular alkyl, low molecular alkoxy and sulpho groups or are unsubstituted; phenols which are substituted by low molecular dialkylamino groups, by acylamino groups and by alkyl groups of 1 to 5 carbon atoms, and which couple in ortho-position; 2,6-dihydroxy-3-cyano- or 2,6-dihydroxy-3-carbonamido-4-alkylpyridines and 6-hydroxy-2-pyridones which are substituted in 1-position by low molecular, substituted or unsubstituted alkyl, e.g. methyl, isopropyl, .beta.-hydroxyethyl, .beta.-aminoethyl, .gamma.-isopropoxypropyl or by -NH.sub.2 or a substituted amino group, e.g. dimethylamino or diethylamino, and which carry in 3-position a cyano or carbonamido group and in 4-position a low molecular alkyl group, especially methyl; 5-pyrazolones or 5-aminopyrazolones which have in 1-position a phenyl or naphthyl radical which is substituted by chlorine, nitro, low molecular alkyl and alkoxy groups or is unsubstituted; acetoacetic anilides which are substituted in the anilide nucleus by low molecular alkyl and alkoxy groups, sulphonic acid groups and halogen, especially chlorine, or are unsubstituted; 2,4-diamino- 5-carbonamido-pyridines or 2,4-diamino-5-cyano-pyridines which carry in 6-position a substituted or an unsubstituted amino group, e.g. a phenylamino, sulphophenylamino, pyrrolidino, piperidino, morpholino group or a low molecular alkyl or dialkylamino group.

The term "acylamino" denotes herein amino groups which are substituted by acyl radicals of aliphatic or aromatic sulphonic and, in particular, carboxylic acids or of carbonic acid monoalkyl or monoaryl esters. The term "acyl" therefore encompasses low molecular alkanoyl, alkoxycarbonyl and alkylsulphonyl groups, such as the acetyl, chloroacetyl, propionyl, butyryl, methoxycarbonyl, ethoxycarbonyl, methylsulphonyl or ethylsulphonyl groups, as well as aroyl, aryloxycarbonyl and arylsulphonyl groups, e.g. the benzoyl, chlorobenzoyl, methylbenzoyl, nitrobenzoyl, phenoxycarbonyl, phenylsulphonyl or p-methylsulphonyl group. Preferred acylamino groups are low molecular alkanoylamino, alkoxycarbonylamino or unsubstituted or substituted benzoylamino groups.

Examples of suitable coupling components are:

2-naphthol

1-acetylamino-7-naphthol,

1-propionylamino-7-naphthol,

1-carbomethoxyamino-7-naphthol,

1-carboethoxyamino-7-naphthol,

1-carbopropoxy-amino-7-naphthol,

1-dimethylaminosulphonyl-amino-7-naphthol,

1-naphthol,

5-chloro-1-naphthol,

5,8-dichloro-1-naphthol,

resorcinol,

1-naphthol-3-, -4-, or -5-sulphonic acid,

2-naphthol-3-, -4-, -5-, -6-, -7- or -8-sulphonic acid,

2-naphthol-3-N-(o-sulphophenyl)-carbonamide,

2-naphthol-6-N-(p-sulphophenyl)-sulphonamide,

4-methylphenol,

3-dialkylaminophenol, especially 3-dimethylamino- and 3-diethylaminophenol,

4-t-butylphenol,

4-t-amylphenol,

2- or 3-acetylamino-4-methylphenol,

2-methoxycarbonylamino-4-methylphenol,

2-ethoxycarbonylamino-4-methylphenol,

3,4-dimethylphenol and 2,4-dimethylphenol,

2,6-dihydroxy-3-cyano-4-methylpyridine,

1-methyl-3-cyano-4-ethyl-6-hydroxypyridone-(2),

1-ethyl-3-cyano-4-methyl-6-hydroxypyridone-(2),

1-phenyl-3-carbonamido-4-methyl-6-hydroxypyridone-(2),

1,3-dimethylpyrazolone, pyrazolimine,

1-phenyl-3-methyl-5-pyrazolone,

1-(2'-, 3'- or 4'-methylphenyl)-3-methyl-5-pyrazolone,

1-(2'-methoxyphenyl)-3-methyl-5-pyrazolone,

1-(2'-, 3'- or 4'-chlorophenyl)-3-methyl-5-pyrazolone,

1-(2'-, 3'- or 4'-nitrophenyl)-3-methyl-5-pyrazolone,

1-(2'-, 5'- or 3', 4'-dichlorophenyl)-3-methyl-5-pyrazolone,

1-(2'- 3'- or 4'-sulphophenyl)-3-methyl-5-pyrazolone,

acetoacetic anilide

acetoacetic-o-anisidide,

acetoacetic-o-toluidide,

acetoacetic-o-chloroanilide,

acetoacetic anilide-3- or -4-sulphonic acid,

acetoacetic-m-xylidide,

2,4-dioxyquinoline,

2,4-diamino-5-cyano-6-piperidino-pyridine,

2,4-diamino-5-cyano-6-phenylamino-pyridine.

The azomethine dyes of the formula (1) are manufactured by condensing in known manner the aromatic amines listed hereinbefore from which the radical D is derived with o-hydroxybenzaldehydes or o-hydroxynaphthaldehydes.

Examples of suitable aldehydes are:

2-hydroxybenzaldehyde,

3- and 5-methyl-2-hydroxybenzaldehyde,

3,5- and 3,6-dimethyl-2-hydroxybenzaldehyde,

3-methyl-5-tert.-butyl-2-hydroxybenzaldehyde,

5-chloro- or -bromo-2-hydroxybenzaldehyde,

3- and 4-chloro-2-hyroxybenzaldehyde,

3,5-dichloro-2-hydroxybenzaldehyde,

3-chloro-5-methyl-2-hydroxybenzaldehyde,

3-methyl-5-chloro-2-hydroxybenzaldehyde,

3- and 4- and 5-nitro-2-hydroxybenzaldehyde,

3,5-dinitro- and 4-chloro-5-nitro-2-hydroxybenzaldehyde,

4-methoxy-2-hydroxybenzaldehyde,

1-hydroxy-2-naphthaldehyde and the derivatives thereof which is chlorinated in 4-position; and 2-hydroxy-1-naphthaldehyde.

Among the copper complexes of azo dyes of the formula (8), importance attaches above all to those of the formula ##STR5## wherein p, R.sub.1, R.sub.2 and M have the meanings already assigned to them and E' is the radical of a naphthol which is substituted by chlorine, bromine, acylamino, sulpho, low molecular alkyl and alkoxy or is unsubstituted, the radical of a phenol which is substituted by low molecular dialkylamino groups, alkylamino groups or alkyl of 1 to 5 carbon atoms, the radical of a 1-aryl-3-methyl-5-pyrazolone, a 3-cyano- or 3-carbonamido-4-methyl-6-hydroxy-pyridone-2, a 2,4-diamino-5-cyanopyridine or 2,4-diamino-5-carbonamidopyridine or of an acetoacetic anilide.

Preferably p is 1 and R.sub.1 is hydrogen or methyl. The following compounds are to be singled out for special mention as important coupling components from which E' is derived: naphthols of the formulae ##STR6## wherein Z is a hydrogen atom or an acylamino group and each of Z.sub.1 and Z.sub.2 is independently hydrogen or chlorine, or wherein Z.sub.1 is a hydrogen atom and Z.sub.2 is a sulpho group; pyridones of the formula ##STR7## wherein Z.sub.3 is an alkyl radical of 1 to 4 carbon atoms which is substituted by OH, NH.sub.2 or a low molecular alkoxy group or is unsubstituted and Z.sub.4 is the CN or the CONH group.

The novel metal complexes are manufactured by methods which are known per se in an aqueous or organic medium. Copper, nickel, chromium and cobalt salts, e.g. copper sulphate, copper nitrate, nickel sulphate, chromium(III) chloride, cobalt sulphate and cobalt acetate are used as metal donors. It is also possible to use the freshly precipitated hydroxides. The reaction is carried out in a weekly acid to alkaline range. It is carried out for example with copper sulphate in aqueous medium in the presence of sodium acetate or ammonia or with copper nitrate in the presence of sodium carbonate in an organic medium, such as cellosolve.

Ordinarily the reaction is carried out with heating, e.g. at a temperature somewhat below the boiling point of the solvent used.

The novel dyes are suitable for dyeing and printing natural or synthetic polyamide materials, such as wool or especially nylon. The dyeing is carried out in aqueous dyebaths at pH values 4 to 8.

The dyeings obtained with the novel dyes are characterised by purity, depth and brilliance of shade. Their fastness properties, such as fastness to washing, rubbing, water, alkali and acid, are generally good and their light fastness is exceptional. The dyeings are also very level, since the novel dyes cover barriness on nylon well.

The invention is illustrated by the following Examples in which the parts are by weight.

EXAMPLE 1 ##STR8##

10.4 parts of the dye obtained by acid coupling of diazotised 2-amino-1-oxy-benzene-4-(2'-sulphonic acid)-sulphanilide with 3-diethylamino-1-oxybenzene are dissolved in 400 parts of water by addition of sodium hydroxide at pH 7 and the solution is heated to 70.degree. C. A solution of 6 parts of copper sulphate crystals in 30 parts of water is added dropwise at 70.degree.-75.degree. C. and the pH is kept at 4-5 by addition of a 4 normal sodium acetate solution. Upon termination of the reaction, the completely precipitated dye is filtered off with suction and dried. The product is a red powder which dissolves in water to give a red solution and dyes polyamide and leather in a weakly acid bath in red shades of good fastness properties.

EXAMPLE 2 ##STR9##

6.88 parts of 2-amino-1-oxybenzene-4-(2'-sulphonicacid)-sulphanide and 3.85 parts of 6-methyl-4-tert. butylsalicylaldehyde and 6 parts of copper sulphate crystals are heated in 400 parts of water to 70.degree.-75.degree. C. and the pH is adjusted to 4.5 with sodium acetate. The reaction is terminated after the mixture has been stirred for 4 hours. The completely precipitated dye is isolated by filtration and then dried. It is a yellow powder which dissolves in water to give a yellow solution and dyes polyamide and leather in a weakly acid bath in yellow shades of good fastness to light and wet treatments.

EXAMPLE 3 ##STR10##

49.3 parts of the dye obtained by coupling diazotised 2-amino-1-oxybenzene-4-sulphanilide-2'-sulphonic acid with 2-naphthol are dissolved in 1000 parts of water. The solution is heated to 70.degree. C. and adjusted to pH 5.0 with acetic acid. Upon addition of a solution of an amount of copper sulphate (containing 7 parts of copper) in 100 parts of water, the pH is adjusted to 4.5 by addition of sodium acetate and the reaction mixture is stirred for 1 hour at 70.degree.-75.degree. C. Upon termination of the reaction the dye is filtered off and dried. It is a dark red powder which dissolves in water to give a red solution and dyes polyamides in bluish red shades of good fastness properties.

Further dyes which also have good fastness properties are obtained in analogous manner by reacting the dyes of column I of the table with the metal atoms listed in column II in the ratio indicated in column III.

__________________________________________________________________________ Shade on I II III polyamide __________________________________________________________________________ ##STR11## Cu 1:1 reddish yellow " Ni 1:1 yellow ##STR12## Cu 1:1 yellow " Ni 1:1 pale yellow " Co 2:1 yellow ##STR13## Cu 1:1 brown ##STR14## Cu 1:1 reddish violet " Ni 1:1 violet ##STR15## Ni 1:1 yellowish claret ##STR16## Cu 1:1 violet ##STR17## Cu 1:1 orange ##STR18## Cu 1:1 bluish red ##STR19## Cu 1:1 violet ##STR20## Cu 1:1 bluish violet ##STR21## Cu 1:1 reddish brown ##STR22## Cu 1:1 reddish brown ##STR23## Cu 1:1 bluish red ##STR24## Cu 1:1 bluish red ##STR25## Cu 1:1 bluish red ##STR26## Cu 1:1 reddish violet ##STR27## Cu 1:1 greyish blue ##STR28## Cu 1:1 violet ##STR29## Cu 1:1 violet ##STR30## Cu 1:1 bluish violet ##STR31## Cu 1:1 violet ##STR32## Cu 1:1 bluish violet ##STR33## Cu 1:1 yellow ##STR34## Cu 1:1 blue ##STR35## Cu 1:1 yellow ##STR36## Cu 1:1 yellow " Ni 1:1 golden yellow ##STR37## Cu 1:1 reddish brown ##STR38## Ni 1:1 orange ##STR39## Cu 1:1 reddish orange " Ni 1:1 orange ##STR40## Cu 1:1 bluish red " Ni 1:1 brown ##STR41## Cu 1:1 yellow ##STR42## Cu 1:1 yellowish red " Ni 1:1 red " Co 2:1 claret ##STR43## Ni 1:1 red ##STR44## Cu 1:1 yellowish brown " Ni 1:1 reddish orange " Co 2:1 red " Cr 2:1 claret ##STR45## Co 2:1 reddish brown ##STR46## Cu 1:1 orange " Ni 1:1 reddish orange " Co 2:1 scarlet " Cr 2:1 claret ##STR47## Cu 1:1 orange " Ni 1:1 orange " Cr 2:1 claret " Co 2:1 red ##STR48## Cu 1:1 orange " Ni 1:1 yellow orange " Cr 2:1 claret " Co 2:1 red ##STR49## Cu 1:1 greenish yellow " Ni 1:1 yellow ##STR50## Ni 1:1 brownish orange ##STR51## Cu 1:1 violet ##STR52## Cu 1:1 yellow ##STR53## Co 2:1 brown ##STR54## Cu 1:1 reddish brown ##STR55## Cu 1:1 violet " Ni 1:1 claret ##STR56## Ni 1:1 reddish orange ##STR57## Cu 1:1 yellow ##STR58## Cu 1:1 reddish blue ##STR59## Cu 1:1 grey ##STR60## Cu 1:1 brownish grey ##STR61## Cu 1:1 yellowish brown ##STR62## Cu 1:1 violet brown ##STR63## Cu 1:1 yellowish brown ##STR64## Cu 1:1 greenish blue ##STR65## Cu 1:1 red ##STR66## Cu 1:1 orange ##STR67## Cu 1:1 yellow " Ni 1:1 yellow ##STR68## Ni 1:1 red ##STR69## Ni 1:1 reddish brown " Co 2:1 greenish grey ##STR70## Ni 1:1 reddish violet ##STR71## Cu 1:1 yellowish brown __________________________________________________________________________

Claims

1. A copper, nickel, chromium or cobalt complex of a dye of the formula

2. A copper, nickel, chromium or cobalt complex of claim 1, wherein Z is --SO.sub.2 -- and U is --SO.sub.3 M, wherein M is hydrogen, an alkali metal or ammonium.

3. The compound of the formula: ##STR72##

4. The compound of the formula: ##STR73##